Canonical Allele Identifier: CA915945660
Gene: PLAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42179964_42179966delinsATA , CM000670.2:g.42179964_42179966delinsATA GRCh38
NC_000008.10:g.42037482_42037484delinsATA , CM000670.1:g.42037482_42037484delinsATA GRCh37
NC_000008.9:g.42156639_42156641delinsATA NCBI36
NG_023264.1:g.32711_32713delinsTAT , LRG_570:g.32711_32713delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000220809.9:c.1323_1325delinsTAT MANE Select ENSP00000220809.4:p.Trp441_Thr442delinsCysMet
ENST00000677722.1:n.2261_2263delinsTAT
ENST00000678083.1:c.*160_*162delinsTAT ENSP00000504824.1:n.*160_*162delinsTAT
ENST00000678676.1:c.*682_*684delinsTAT ENSP00000502858.1:n.*682_*684delinsTAT
ENST00000679151.1:c.1323_1325delinsTAT ENSP00000504311.1:p.Trp441_Thr442delinsCysMet
ENST00000679300.1:c.1323_1325delinsTAT ENSP00000503050.1:p.Trp441_Thr442delinsCysMet
ENST00000220809.8:c.1323_1325delinsTAT ENSP00000220809.4:p.Trp441_Thr442delinsCysMet
ENST00000352041.7:c.1185_1187delinsTAT ENSP00000270188.6:p.Trp395_Thr396delinsCysMet
ENST00000429089.6:c.1323_1325delinsTAT ENSP00000392045.2:p.Trp441_Thr442delinsCysMet
ENST00000429710.6:c.945_947delinsTAT ENSP00000407861.2:p.Trp315_Thr316delinsCysMet
ENST00000519510.5:c.1134_1136delinsTAT ENSP00000428886.1:p.Trp378_Thr379delinsCysMet
ENST00000524009.5:c.1056_1058delinsTAT ENSP00000429401.1:p.Trp352_Thr353delinsCysMet
NM_000930.3:c.1323_1325delinsTAT , LRG_570t1:c.1323_1325delinsTAT NP_000921.1:p.Trp441_Thr442delinsCysMet
NM_033011.2:c.1185_1187delinsTAT NP_127509.1:p.Trp395_Thr396delinsCysMet
NM_000930.4:c.1323_1325delinsTAT NP_000921.1:p.Trp441_Thr442delinsCysMet
NM_001319189.1:c.1056_1058delinsTAT NP_001306118.1:p.Trp352_Thr353delinsCysMet
NM_033011.3:c.1185_1187delinsTAT NP_127509.1:p.Trp395_Thr396delinsCysMet
NM_000930.5:c.1323_1325delinsTAT MANE Select NP_000921.1:p.Trp441_Thr442delinsCysMet
NM_001319189.2:c.1056_1058delinsTAT NP_001306118.1:p.Trp352_Thr353delinsCysMet
NM_033011.4:c.1185_1187delinsTAT NP_127509.1:p.Trp395_Thr396delinsCysMet
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